周孝钱,许俊,唐江琼,秦旭平.CGRP对氧化损伤人脐静脉内皮细胞的保护作用及Caveolin-1表达的影响.[J].中南医学科学杂志.,2011,39(2):131-134.
CGRP对氧化损伤人脐静脉内皮细胞的保护作用及Caveolin-1表达的影响
Effect of CGRP on Protection of Human Umbilical Vein Endothelial Cells and Caveolin-1 Expression Induced by H2O2
投稿时间:2010-11-24  
DOI:
中文关键词:  过氧化氢  CGRP  Caveolin-1  内皮细胞  动脉粥样硬化
英文关键词:H2O2  CGRP  Caveolin-1  hUVECs  atherosclerosis
基金项目:国家自然科学基金资助(30572192)及南华大学学术带头人培养对象资金资助.
作者单位
周孝钱,许俊,唐江琼,秦旭平 南华大学 药物药理研究所湖南 衡阳 421001 
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中文摘要:
      目的探讨降钙素基因相关肽(CGRP)对过氧化氢(H2O2)诱导离体培养的人脐静脉内皮细胞(hUVECs)损伤的保护作用及其机制。方法CGRP预孵育hUVECs后,用不同浓度H2O2处理hUVECs,噻唑蓝比色法(MTT)观察hUVECs活性;Western-blot检测Caveolin-1表达。结果CGRP(0.1~100.0 nmol/L)能呈浓度依赖性提高hUVECs活性。H2O2(0.2~5.0 mmol/L)能呈浓度依赖性降低hUVECs活性。CGRP(10~100 nmol/L)预孵育hUVECs 30 min能明显提高H2O2诱导的hUVECs抗损伤能力(P﹤0.05);与0.1%FBS组比较,100 nmol/L CGRP和0.05 mmol/L H2O2处理组细胞Caveolin-1蛋白水平表达下降(P﹤0.05);0.8 mmol/L H2O2处理组细胞Caveolin-1蛋白表达水平上升(P﹤0.05);与H2O2处理组比较,100 nmol/L CGRP预孵育hUVECs 30 min能显著降低细胞Caveolin-1蛋白水平的表达(P﹤0.05)。结论CGRP对H2O2诱导的hUVECs损伤有一定的保护作用,其机制可能与下调氧化应激导致的hUVECs Caveolin-1的表达有关。
英文摘要:
      ObjectiveTo study the protective effect of cacitonin gene-related peptide (CGRP) on human umbilical vein endothelial cells (hUVECs) injury induced by H2O2 and the related mechanism of action.MethodsCGRP and/or H2O2 were used for treatment of hUVECs.Cell viability was determined by methyl thiazolyltetrazolium (MTT) assay.Expression of Caveolin-1 was measured by Western-blot.ResultsCGRP(0.1~100.0 nmol/L)could dose-dependently induce the cell viability of hUVECs.H2O2(0.2~5.0 mmol/L)could dose-dependently impaire the cell viability of hUVECs.Pretreatment of hUVECs 30min with CGRP(10~100 nmol/L)dose-dependently increased the cell viability impaired by H2O2.Compared with 0.1%FBS group,100 nmol/L CGRP and 0.05 mol/L H2O2 down-regulated the expression of Caveolin-1,which was up-regulation of incubation of 0.8 mmol/L of H2O2.Compared with H2O2 group,the expression of Caveolin-1 was significantly decreased by pretreatment with CGRP.ConclusionCGRP has a protective effect on the hUVECs injured by H2O2;the mechanism may be related to decreasing the expression of Caveolin-1.
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